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Quality Systems Manager job in Essex

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Job Ref:  204268437
Employer:  cv-library.co.uk
Industry:  Civil and Structural
Job Type:  Permanent
Country:  United Kingdom
County/State:  Essex
City:  Essex
Post Code:  SS14
10/10/2016 18:51
As part of the global manufacturing community, our client manufacturing centre plays a key role in the development and manufacture of new, sophisticated medical and industrial products. Working with colleagues in Europe, the USA and Japan, engineers is fully equipped with the latest technologies, to enable them to develop medical products & accessories, and industrial devices. Our client Produces world class products in terms of Quality, Cost and Delivery, it's essential. Therefore, in today's fast moving, ever changing world, we continue to invest in both our people and the latest equipment and processes to remain at the forefront in manufacturing technology.
Your Responsibilities:
Participate in the design and manufacturing process to ensure products meet SQCD requirements.
Deputise for the Quality Management Systems Representative.
Assures that quality systems procedures, processes, practices and controls are properly developed, implemented and maintained.
Assures that all products represent the maximum quality and reliability attainable.
Routinely provides guidance and leadership to engineers, inspectors and/or technicians for the duration of a project assignment.
Key role in ensuring product issues are promptly investigated and adequate corrective/preventive action implemented e.g. customer complaints, out of specification components, etc.
Ensures the CAPA systems are operating effectively and close out of corrective actions meets expected deadlines.

Your Qualifications

Degree, or equivalent, in an Engineering or Life-Sciences Discipline.
Five years experience in a Quality Systems and/or Engineering role within an Electro-Mechanical or Electronics or Sterile Medical Devices Manufacturing environment.
Experience in a Medical Device facility and knowledge of FDA Quality System Regulations (21 CFR 820), EU MDD, JPAL, ISO13485 and ISO9001.
Proven track record in a supervisory role
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